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Study profile: the Genetics of Glaucoma Study

PURPOSE: Glaucoma, a major cause of irreversible blindness, is a highly heritable human disease. Currently, the majority of the risk genes for glaucoma are unknown. We established the Genetics of Glaucoma Study (GOGS) to identify disease genes and improve genetic prediction of glaucoma risk and resp...

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Autores principales: Gharahkhani, Puya, He, Weixiong, Diaz Torres, Santiago, Wu, Yeda, Ingold, Nathan, Yu, Regina, Seviiri, Mathias, Ong, Jue-Sheng, Law, Matthew H, Craig, Jamie E, Mackey, David A, Hewitt, Alex W, MacGregor, Stuart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401214/
https://www.ncbi.nlm.nih.gov/pubmed/37536973
http://dx.doi.org/10.1136/bmjopen-2022-068811
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author Gharahkhani, Puya
He, Weixiong
Diaz Torres, Santiago
Wu, Yeda
Ingold, Nathan
Yu, Regina
Seviiri, Mathias
Ong, Jue-Sheng
Law, Matthew H
Craig, Jamie E
Mackey, David A
Hewitt, Alex W
MacGregor, Stuart
author_facet Gharahkhani, Puya
He, Weixiong
Diaz Torres, Santiago
Wu, Yeda
Ingold, Nathan
Yu, Regina
Seviiri, Mathias
Ong, Jue-Sheng
Law, Matthew H
Craig, Jamie E
Mackey, David A
Hewitt, Alex W
MacGregor, Stuart
author_sort Gharahkhani, Puya
collection PubMed
description PURPOSE: Glaucoma, a major cause of irreversible blindness, is a highly heritable human disease. Currently, the majority of the risk genes for glaucoma are unknown. We established the Genetics of Glaucoma Study (GOGS) to identify disease genes and improve genetic prediction of glaucoma risk and response to treatment. PARTICIPANTS: More than 5700 participants with glaucoma or a family history of glaucoma were recruited through a media campaign and the Australian Government healthcare service provider, Services Australia, making GOGS one of the largest genetic studies of glaucoma globally. The mean age of the participants was 65.30±9.36 years, and 62% were female. Participants completed a questionnaire obtaining information about their glaucoma-related medical history such as family history, glaucoma status and subtypes, surgical procedures, and prescriptions. The questionnaire also obtained information about other eye and systemic diseases. Approximately 80% of the participants provided a DNA sample and ~70% consented to data linkage to their Australian Government Medicare and Pharmaceutical Benefits Scheme schedules. FINDINGS TO DATE: 4336 GOGS participants reported that an optometrist or ophthalmologist has diagnosed them with glaucoma and 3639 participants reported having a family history of glaucoma. The vast majority of the participants (N=4393) had used at least one glaucoma-related medication; latanoprost was the most commonly prescribed drug (54% of the participants who had a glaucoma prescription). A subset of the participants reported a surgical treatment for glaucoma including a laser surgery in 2008 participants and a non-laser operation in 803 participants. Several comorbid eye and systemic diseases were also observed; the most common reports were ocular hypertension (53% of the participants), cataract (48%), hypertension (40%), nearsightedness (31%), astigmatism (22%), farsightedness (16%), diabetes (12%), sleep apnoea (11%) and migraines (10%). FUTURE PLANS: GOGS will contribute to the global gene-mapping efforts as one of the largest genetic studies for glaucoma. We will also use GOGS to develop or validate genetic risk prediction models to stratify glaucoma risk, particularly in individuals with a family history of glaucoma, and to predict clinical outcomes (eg, which medication works better for an individual and whether glaucoma surgery is required). GOGS will also help us answer various research questions about genetic overlap and causal relationships between glaucoma and its comorbidities.
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spelling pubmed-104012142023-08-05 Study profile: the Genetics of Glaucoma Study Gharahkhani, Puya He, Weixiong Diaz Torres, Santiago Wu, Yeda Ingold, Nathan Yu, Regina Seviiri, Mathias Ong, Jue-Sheng Law, Matthew H Craig, Jamie E Mackey, David A Hewitt, Alex W MacGregor, Stuart BMJ Open Ophthalmology PURPOSE: Glaucoma, a major cause of irreversible blindness, is a highly heritable human disease. Currently, the majority of the risk genes for glaucoma are unknown. We established the Genetics of Glaucoma Study (GOGS) to identify disease genes and improve genetic prediction of glaucoma risk and response to treatment. PARTICIPANTS: More than 5700 participants with glaucoma or a family history of glaucoma were recruited through a media campaign and the Australian Government healthcare service provider, Services Australia, making GOGS one of the largest genetic studies of glaucoma globally. The mean age of the participants was 65.30±9.36 years, and 62% were female. Participants completed a questionnaire obtaining information about their glaucoma-related medical history such as family history, glaucoma status and subtypes, surgical procedures, and prescriptions. The questionnaire also obtained information about other eye and systemic diseases. Approximately 80% of the participants provided a DNA sample and ~70% consented to data linkage to their Australian Government Medicare and Pharmaceutical Benefits Scheme schedules. FINDINGS TO DATE: 4336 GOGS participants reported that an optometrist or ophthalmologist has diagnosed them with glaucoma and 3639 participants reported having a family history of glaucoma. The vast majority of the participants (N=4393) had used at least one glaucoma-related medication; latanoprost was the most commonly prescribed drug (54% of the participants who had a glaucoma prescription). A subset of the participants reported a surgical treatment for glaucoma including a laser surgery in 2008 participants and a non-laser operation in 803 participants. Several comorbid eye and systemic diseases were also observed; the most common reports were ocular hypertension (53% of the participants), cataract (48%), hypertension (40%), nearsightedness (31%), astigmatism (22%), farsightedness (16%), diabetes (12%), sleep apnoea (11%) and migraines (10%). FUTURE PLANS: GOGS will contribute to the global gene-mapping efforts as one of the largest genetic studies for glaucoma. We will also use GOGS to develop or validate genetic risk prediction models to stratify glaucoma risk, particularly in individuals with a family history of glaucoma, and to predict clinical outcomes (eg, which medication works better for an individual and whether glaucoma surgery is required). GOGS will also help us answer various research questions about genetic overlap and causal relationships between glaucoma and its comorbidities. BMJ Publishing Group 2023-08-03 /pmc/articles/PMC10401214/ /pubmed/37536973 http://dx.doi.org/10.1136/bmjopen-2022-068811 Text en © Author(s) (or their employer(s)) 2023. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Ophthalmology
Gharahkhani, Puya
He, Weixiong
Diaz Torres, Santiago
Wu, Yeda
Ingold, Nathan
Yu, Regina
Seviiri, Mathias
Ong, Jue-Sheng
Law, Matthew H
Craig, Jamie E
Mackey, David A
Hewitt, Alex W
MacGregor, Stuart
Study profile: the Genetics of Glaucoma Study
title Study profile: the Genetics of Glaucoma Study
title_full Study profile: the Genetics of Glaucoma Study
title_fullStr Study profile: the Genetics of Glaucoma Study
title_full_unstemmed Study profile: the Genetics of Glaucoma Study
title_short Study profile: the Genetics of Glaucoma Study
title_sort study profile: the genetics of glaucoma study
topic Ophthalmology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10401214/
https://www.ncbi.nlm.nih.gov/pubmed/37536973
http://dx.doi.org/10.1136/bmjopen-2022-068811
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